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| Product | Description | |
|---|---|---|
| Praziquantel-d11 | Praziquantel-d11 is the deuterium labeled Praziquantel, which is an anthelmintic. Uses: Scientific research. Category: Signaling pathways. CAS No. 1246343-36-1. Pack Sizes: 500 μg; 1 mg. Product ID: HY-B0244S. |  |
| Praziquantel-d11 | Labeled Praziquantel. Anthelmintic, effective against flatworms. Group: Biochemicals. Alternative Names: 2-(Cyclohexylcarbonyl)-1,2,3,6,7,11b-hexahydro-4H-(pyrazino-d11)[2,1-a]isoquinolin-4-one; (+/-)-Praziquantel-d11; Azinox-d11; Biltricide-d11; Cesol-d11; Cysticide-d11; Distocide-d11; Droncit-d11; Embay 8440-d11; Prazinon-d11; Pyquiton-d11; Warmnil-d11. Grades: Highly Purified. CAS No. 1246343-36-1. Pack Sizes: 2.5mg. US Biological Life Sciences. |  Worldwide |
| Praziquantel-[d11] | Praziquantel-[d11] is the labelled analogue of Praziquantel. Praziquantel can be used for the treatment of a number of types of parasitic worm infections. Specifically it is used for schistosomiasis, clonorchiasis, opisthorchiasis, tapeworm infections, cysticercosis, hydatid disease, and other fluke infections. Uses: The d11 isotope labelled praziquantel. Synonyms: Praziquantel-d11; 2-(Cyclohexylcarbonyl)-1,2,3,6,7,11b-hexahydro-4H-(pyrazino-d11)[2,1-a]isoquinolin-4-one. Grade: 95% by HPLC; 95% atom D. CAS No. 1246343-36-1. Molecular formula: C19H13D11N2O2. Mole weight: 323.47. |  |
| Praziquantel EP Impurity A | Praziquantel EP Impurity A. Uses: For analytical and research use. CAS No. 54761-87-4. Molecular formula: C19H18N2O2. Mole weight: 306.37. Catalog: APB54761874. |  |
| Praziquantel EP Impurity B | Praziquantel EP Impurity B. Uses: For analytical and research use. CAS No. 125273-86-1. Molecular formula: C19H22N2O2. Mole weight: 310.4. Catalog: APB125273861. | |
| Praziquantel EP Impurity C | Praziquantel EP Impurity C. Uses: For analytical and research use. CAS No. 125273-88-3. Molecular formula: C19H22N2O4. Mole weight: 342.4. Catalog: APB125273883. | |
| Praziquantel Impurity 1 | Praziquantel Impurity 1. Uses: For analytical and research use. CAS No. 60743-58-0. Molecular formula: C19H24N2O3. Mole weight: 328.41. Catalog: APB60743580. | |
| Praziquantel Related Compound A | Praziquantel Related Compound A. Uses: For analytical and research use. CAS No. 54761-87-4. Mole weight: 306.36. Catalog: AP54761874. | |
| Praziquantel Related Compound B | Praziquantel Related Compound B. Uses: For analytical and research use. CAS No. 125273-86-1. Mole weight: 310.39. Catalog: AP125273861. | |
| Praziquantel Related Compound C | Praziquantel Related Compound C. Uses: For analytical and research use. CAS No. 125273-88-3. Mole weight: 342.39. Catalog: AP125273883. | |
| Prazobind | Prazobind. Group: Biochemicals. Alternative Names: 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-bicyclo[2.2.2]octa-2,5-dienyl-carbonyl)-piperazine; SZL-49. Grades: Highly Purified. CAS No. 107021-36-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C23H27N5O3. US Biological Life Sciences. | Worldwide |
| Prazobind-d8 | α1-Adrenoceptor alkylating reagent. A labeled Prazosin analog. Group: Biochemicals. Alternative Names: 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-bicyclo[2.2.2]octa-2,5-dienyl-carbonyl)-(piperazine-d8); SZL-49-d8. Grades: Highly Purified. CAS No. 1189701-23-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Prazobind-[d8] | Prazobind-[d8] is the labelled analogue of Prazobind. Prazobind is an α1-adrenergic receptor (AR) antagonist. Uses: Α1-adrenoceptor alkylating reagent. a labelled prazosin analog. Synonyms: Prazobind D8; 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-bicyclo[2.2.2]octa-2,5-dienyl-carbonyl)-(piperazine-d8). Grade: 95% by HPLC; 95% atom D. CAS No. 1189701-23-2. Molecular formula: C23H19D8N5O3. Mole weight: 429.54. | |
| Prazosin | Prazosin is an α-adrenergic receptor antagonist. Prazosin can reduce inflammation, relieve anxiety, alleviate panic, prevent memory decline, and modulate the pain-relieving effects of opioids. Prazosin can be used in the study of hypertension and Alzheimers disease[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 19216-56-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-B0193. | |
| Prazosin-d8 | Labeled Prazosin. An antihypertensive. α1-Adrenergic blocker. Group: Biochemicals. Alternative Names: 4-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-1-piperazinyl-d8]-2-furanylmethanone; 1- (4-Amino-6, 7-dimethoxy-2-quinazolinyl) -4- (2-furanylcarbonxyl) piperazine-d8; Adversuten-d8; Adverszuten-d8; Alpress LP-d8. Grades: Highly Purified. CAS No. 1006717-55-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Prazosin-[d8] | An isotope labelled Prazosin. Prazosin is an inverse agonist at alpha-1 adrenergic receptor. Prazosin is a sympatholytic drug used to treat high blood pressure, anxiety, and posttraumatic stress disorder (PTSD). Synonyms: 4-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-1-piperazinyl-d8]-2-furanylmethanone; 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-furanylcarbonxyl) piperazine-d8; Adversuten-d8; Adverszuten-d8; Alpress LP-d8; Furazosin-d8; Lentopres-d8; NSC 292810-d8; Peripress-d8. Grade: >95%. CAS No. 1006717-55-0. Molecular formula: C19H13D8N5O4. Mole weight: 391.46. | |
| Prazosin hydrochloride | Prazosin hydrochloride is a well-tolerated, CNS-active α1-adrenergic receptor antagonist for the research of high blood pressure and alcohol use disorders[1]. Prazosin hydrochloride potently inhibits Norepinephrine (NE)-stimulated 45Ca efflux with an IC50 of 0.15 nM[2].Prazosin hydrochloride inhibits organic cation transporters OCT-1 and OCT-3 with IC50s of 1.8, and 13 μM, respectively[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 19237-84-4. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 200 mg; 500 mg. Product ID: HY-B0193A. | |
| Prazosin hydrochloride | Prazosin hydrochloride. Uses: For analytical and research use. CAS No. 19237-84-4. Mole weight: 419.86. Catalog: AP19237844-A. | |
| Prazosin Hydrochloride | Prazosin Hydrochloride (Terazosin EP Impurity K) is an antihypertensive. α1-Adrenergic blocker. Prazosin hydrochloride, a quinazole derivative, is a very potent and highly selective antagonist for apha-1-adrenoceptors (affinity for alpha-1 is about 1000-fold greater than for alpha-2 receptors). Mainly used as a clinic vasodilator for blood pressure control without increasing the heart rate or significantly impairing sympathetic functions. Has also been used clinically to treat anxiety, PTSD, and panic disorder. An excellent candidate for research studying brain functions mediated through alpha-1-adrenergic receptors, such as reward, pleasure, aggression, fear, anxiety, and addiction. Group: Biochemicals. Alternative Names: [4-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-1-piperazinyl]-2-furanylmethanone Hydrochloride; 1- (4-Amino-6, 7-dimethoxy-2-quinazolinyl) -4- (2-furanylcarbonxyl) piperazine Hydrochloride; Adversuten; Adverszuten; Alpress LP; Furazosin; Lentopres; NSC 292810; Peripress; Terazosin EP Impurity K. Grades: Highly Purified. CAS No. 19237-84-4. Pack Sizes: 100mg, 250mg, 500mg. Molecular Formula: C??H??ClN?O?, Molecular Weight: 419.86r. US Biological Life Sciences. | Worldwide |
| PR-bombesin | PR-bombesin is an antimicrobial peptide found in Bombina maxima (Chinese red belly toad), and has antimicrobial activity as some neuropeptides. Synonyms: Glu-Lys-Lys-Pro-Pro-Arg-Pro-Pro-Gln-Trp-Ala-Val-Gly-His-Phe-Met; proline rich bombesin-related peptide (PR-bombesin). Grade: ≥97%. Molecular formula: C89H133N25O20S. Mole weight: 1905.26. | |
| PRC1-IN-1 | PRC1-IN-1 is a PRC1 complex inhibitor. PRC1-IN-1 binds to both RING1A and RING1B proteins, and inhibits the activities of RING1B-BMI1 and RING1B-PCGF1. PRC1-IN-1 effectively inhibits H2AK119 ubiquitination and induces cell differentiation in leukemia cells. PRC1-IN-1 can be used for the research of leukemia[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2396639-29-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-170823. | |
| pRc/CMV HBS Liposome | This liposome contains pRc/CMV HBS, which increases the level of secretory immunoglobulin IgA. It is only for research purposes. Group: Liposomal vaccine or adjuvant. |  |
| PrDiAzK | PrDiAzK is a bifunctional amino acid. PrDiAzK can be site-selectively incorporated into proteins in both bacterial and mammalian cell culture. PrDiAzK can be used for proteome-wide incorporation via stochastic orthogonal recoding of translation (SORT)[1]. PrDiAzK is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 2231405-64-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-132975. | |
| PRDX1-IN-1 | PRDX1-IN-1 is a selective inhibtor of PRDX1 with an IC50 value of 0.164 μM. PRDX1-IN-1 can be used in researches related to cancer.PRDX1-IN-1 promots intracellular ROS accumulation, and inhibits the proliferation, invasion and migration of cancer cells besides inducing apoptosis. PRDX1-IN-1 could be used in cancer research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2996096-63-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-149394. | |
| PRE-084 hydrochloride | PRE-084 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 138847-85-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| PRE-084 hydrochloride | PRE-084 hydrochloride is a highly selective σ1 receptor (S1R) agonist, with an IC50 of 44 nM. PRE-084 hydrochloride exhibits good neuroprotective effects, can improve motor function and motor neuron survival in mice. PRE-084 hydrochloride also can ameliorate myocardial ischemia-reperfusion injury in rats by activating the Akt-eNOS pathway[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 75136-54-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-18100A. | |
| pre-calcitriol PTAD adduct | pre-calcitriol PTAD adduct. Group: Biochemicals. Alternative Names: [4aR-[4a-a, 6a-a, 7a(R*), 9a-b, 11a(3S*, 5R*)]]-11-(3, 5-Dihydroxy-2-methyl-1-cyclohexen-1-yl)-4a, 6, 6a, 7, 8, 9, 9a, 11-octahydro-7-(5-hydroxy-1, 5-dimethylhexyl)-6a-methyl-2-phenyl-1H, 5H-cyclopenta[f][1, 2, 4]triazolo[1, 2-a]cinnoline-1, 3(2H)-dione. Grades: Highly Purified. CAS No. 86307-44-0. Pack Sizes: 5mg, 10mg. Molecular Formula: C35H49N3O5. US Biological Life Sciences. | Worldwide |
| Pre-Capped White Plastic Ointment Jars | Pre-Capped White Plastic Ointment Jars. Product ID: PM-037. Product Keywords: Packaging Materials; Plastic Packaging; PM-037; Pre-Capped White Plastic Ointment Jars. |  |
| Precemtabart | HY-P990940 is an CEACAM5-targeting IgG1κ type human antibody, the recommed isotype control is Human IgG1 kappa, Isotype Control (HY-P99001)[1]. Uses: Scientific research. Category: Inhibitory antibodies. Alternative Names: MBE-748; M-9140 Antibody; MBE-2882 Antibody. CAS No. 2883118-92-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990940. | |
| Precemtabart tocentecan | Precemtabart tocentecan (Precem-TcT; M 9140) is an anti-CEACAM5 (carcinoembryonic antigen-related cell adhesion molecule 5) antibody-drug conjugate (ADC). Precemtabart tocentecan consists of a tumor-specific anti-CEACAM5 monoclonal antibody Precemtabart (HY-P990940), a highly hydrophilic and stable cleavable β-glucuronide linker, and a topoisomerase 1 inhibitor payload Exatecan (HY-13631), and the drug-linker conjugate for ADC is Mal-Gly-PAB-Exatecan-D-glucuronic acid (HY-153179). Precemtabart tocentecan inhibits the growth of CEACAM5-positive cancer cells. Precemtabart tocentecan exhibits significant antitumor activity in CEACAM5-expressing xenograft models. Precemtabart tocentecan can be used for the study of CEACAM5-expressing advanced solid tumors, especially mCRC[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Precem-TcT; M 9140. CAS No. 2873366-83-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-177434. | |
| Precipitated Calcium Carbonate | Precipitated Calcium Carbonate. |  |
| Precision molds | Precision molds. | |
| Preclinical Compound Library | A unique collection of 709 preclinical compounds for high throughput screening (HTS) and high content screening (HCS); - Hot lead compounds for new drug discovery and development; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - Structurally diverse, medicinally active, and cell permeable; - NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L3410. Categories: Preclinical Compounds Libraries. |  |
| precorrin-2 C20-methyltransferase | This enzyme belongs to the family of transferases, specifically those transferring one-carbon group methyltransferases. The systematic name of this enzyme class is S-adenosyl-L-methionine:precorrin-4 C20-methyltransferase. This enzyme participates in porphyrin and chlorophyll metabolism. Group: Enzymes. Enzyme Commission Number: EC 2.1.1.130. CAS No. 131554-12-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1728; precorrin-2 C20-methyltransferase; EC 2.1.1.130; 131554-12-6. Cat No: EXWM-1728. |  |
| precorrin-2 dehydrogenase | This enzyme catalyses the second of three steps leading to the formation of siroheme from uroporphyrinogen III. The first step involves the donation of two S-adenosyl-L-methionine-derived methyl groups to carbons 2 and 7 of uroporphyrinogen III to form precorrin-2 (EC 2.1.1.107, uroporphyrin-III C-methyltransferase) and the third step involves the chelation of ferrous iron to sirohydrochlorin to form siroheme (EC 4.99.1.4, sirohydrochlorin ferrochelatase). In Saccharomyces cerevisiae, the last two steps are carried out by a single bifunctional enzyme, Met8p. In some bacteria, steps 1-3 are catalysed by a single multifunctional protein called CysG, whereas in Bacillus megaterium, three separate enzymes carry out each of the steps, with SirC being responsible for the above reaction. Group: Enzymes. Synonyms: Met8p; SirC; CysG. Enzyme Commission Number: EC 1.3.1.76. CAS No. 227184-47-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1345; precorrin-2 dehydrogenase; EC 1.3.1.76; 227184-47-6; Met8p; SirC; CysG. Cat No: EXWM-1345. | |
| precorrin-3B C17-methyltransferase | In the aerobic cobalamin biosythesis pathway, four enzymes are involved in the conversion of precorrin-3A to precorrin-6A. The first of the four steps is carried out by EC 1.14.13.83, precorrin-3B synthase (CobG), yielding precorrin-3B as the product. This is followed by three methylation reactions, which introduce a methyl group at C-17 (CobJ; EC 2.1.1.131), C-11 (CobM; EC 2.1.1.133) and C-1 (CobF; EC 2.1.1.152) of the macrocycle, giving rise to precorrin-4, precorrin-5 and precorrin-6A, respectively. Group: Enzymes. Synonyms: precorrin-3 methyltransferase; CobJ. Enzyme Commission Number: EC 2.1.1.131. CAS No. 152787-64-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1729; precorrin-3B C17-methyltransferase; EC 2.1.1.131; 152787-64-9; precorrin-3 methyltransferase; CobJ. Cat No: EXWM-1729. | |
| precorrin-3B synthase | An iron-sulfur protein. An oxygen atom from dioxygen is incorporated into the macrocycle at C-20. In the aerobic cobalamin biosythesis pathway, four enzymes are involved in the conversion of precorrin-3A to precorrin-6A. The first of the four steps is carried out by EC 1.14.13.83, precorrin-3B synthase (CobG), yielding precorrin-3B as the product. This is followed by three methylation reactions, which introduce a methyl group at C-17 (CobJ; EC 2.1.1.131), C-11 (CobM; EC 2.1.1.133) and C-1 (CobF; EC 2.1.1.152) of the macrocycle, giving rise to precorrin-4, precorrin-5 and precorrin-6A, respectively. Group: Enzymes. Synonyms: precorrin-3X synthase; CobG. Enzyme Commission Number: EC 1.14.13.83. CAS No. 152787-63-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0891; precorrin-3B synthase; EC 1.14.13.83; 152787-63-8; precorrin-3X synthase; CobG. Cat No: EXWM-0891. | |
| precorrin-4 C11-methyltransferase | In the aerobic cobalamin biosythesis pathway, four enzymes are involved in the conversion of precorrin-3A to precorrin-6A. The first of the four steps is carried out by EC 1.14.13.83, precorrin-3B synthase (CobG), yielding precorrin-3B as the product. This is followed by three methylation reactions, which introduce a methyl group at C-17 (CobJ; EC 2.1.1.131), C-11 (CobM; EC 2.1.1.133) and C-1 (CobF; EC 2.1.1.152) of the macrocycle, giving rise to precorrin-4, precorrin-5 and precorrin-6A, respectively. Group: Enzymes. Synonyms: precorrin-3 methylase; CobM. Enzyme Commission Number: EC 2.1.1.133. CAS No. 152787-65-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1731; precorrin-4 C11-methyltransferase; EC 2.1.1.133; 152787-65-0; precorrin-3 methylase; CobM. Cat No: EXWM-1731. | |
| precorrin-6A reductase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-CH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is precorrin-6B:NADP+ oxidoreductase. Other names in common use include precorrin-6X reductase, and precorrin-6Y:NADP+ oxidoreductase. This enzyme participates in porphyrin and chlorophyll metabolism. Group: Enzymes. Synonyms: precorrin-6X reductase; precorrin-6Y:NADP+ oxidoreductase. Enzyme Commission Number: EC 1.3.1.54. CAS No. 137573-72-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1325; precorrin-6A reductase; EC 1.3.1.54; 137573-72-9; precorrin-6X reductase; precorrin-6Y:NADP+ oxidoreductase. Cat No: EXWM-1325. | |
| precorrin-6A synthase (deacetylating) | In the aerobic cobalamin biosythesis pathway, four enzymes are involved in the conversion of precorrin-3A to precorrin-6A. The first of the four steps is carried out by EC 1.14.13.83, precorrin-3B synthase (CobG), yielding precorrin-3B as the product. This is followed by three methylation reactions, which introduce a methyl group at C-17 (CobJ; EC 2.1.1.131), C-11 (CobM; EC 2.1.1.133) and C-1 (CobF; EC 2.1.1.152) of the macrocycle, giving rise to precorrin-4, precorrin-5 and precorrin-6A, respectively. Group: Enzymes. Synonyms: precorrin-6X synthase (deacetylating); CobF. Enzyme Commission Number: EC 2.1.1.152. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1748; precorrin-6A synthase (deacetylating); EC 2.1.1.152; precorrin-6X synthase (deacetylating); CobF. Cat No: EXWM-1748. | |
| precorrin-6B C5,15-methyltransferase (decarboxylating) | The enzyme, which participates in the aerobic adenosylcobalamin biosynthesis pathway, has S-adenosyl-L-methionine-dependent methyltransferase and decarboxylase activities. The enzyme is a fusion protein with two active sites; one catalyses the methylation at C15 and the decarboxylation, while the other catalyses the methylation at C5. Group: Enzymes. Synonyms: precorrin-6 methyltransferase; precorrin-6Y methylase; precorrin-6Y C5,15-methyltransferase (decarboxylating); cobL (gene name). Enzyme Commission Number: EC 2.1.1.132. CAS No. 162995-22-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1730; precorrin-6B C5,15-methyltransferase (decarboxylating); EC 2.1.1.132; 162995-22-4; precorrin-6 methyltransferase; precorrin-6Y methylase; precorrin-6Y C5,15-methyltransferase (decarboxylating); cobL (gene name). Cat No: EXWM-1730. | |
| precorrin-8X methylmutase | The enzyme catalyses the the conversion of precorrin-8X to hydrogenobyrinate by methyl rearrangement, a step in the aerobic (late cobalt insertion) pathway of adenosylcobalamin biosynthesis. The equivalent enzyme in the anaerobic pathway is EC 5.4.99.60, precorrin-8 methylmutase. Group: Enzymes. Synonyms: precorrin isomerase; hydrogenobyrinic acid-binding protein; cobH (gene name). Enzyme Commission Number: EC 5.4.99.61. CAS No. 138238-71-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5604; precorrin-8X methylmutase; EC 5.4.99.61; 138238-71-8; precorrin isomerase; hydrogenobyrinic acid-binding protein; cobH (gene name). Cat No: EXWM-5604. | |
| Precyasterone | Precyasterone. Group: Biochemicals. Grades: Plant Grade. CAS No. 27335-85-9. Pack Sizes: 10mg. Molecular Formula: C29H44O8, Molecular Weight: 520.66. US Biological Life Sciences. | Worldwide |
| Prednicarbate | Prednicarbate is a synthetic corticosteroid of the diester class, belonging to the glucocorticoid family of steroidal anti-inflammatory agents. Its structure features a prednisolone skeleton with a 17-propionate and 21-ethyl carbonate esterification, which modulates its topical potency and pharmacokinetic profile. The diesterification contributes to enhanced lipophilicity and targeted local activity with reduced systemic absorption. Applications: Prednicarbate is indicated for the topical treatment of inflammatory and pruritic dermatoses responsive to corticosteroid therapy, including atopic dermatitis, eczematous dermatitis, psoriasis, and allergic contact dermatitis. Category: Active pharmaceutical ingredients. Synonyms: [2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl] propanoate. CAS No. 73771-04-7. Product ID: API73771047. Molecular formula: C27H36O8. Mole weight: 488.6. EINECS: 277-590-3. InChIKey: FNPXMHRZILFCKX-KAJVQRHHSA-N. Appearance: White to off-white solid. |  |
| Prednicarbate | Prednicarbate is a relatively new topical corticosteroid drug. It is similar in potency to hydrocortisone. Corticosteroids have always been an important part of the pharmacological arsenal of dermatology; however, their tendency to produce side-effects has caused the need to search for new preparations. CAS No. 73771-04-7. Product ID: PAP-0074. Molecular formula: C27H36O8. Category: Hormone drug. Product Keywords: Hormone Series; Prednicarbate; PAP-0074; Hormone drug; C27H36O8; 73771-04-7. Standard: USP/EP. Color: White to Off-White. EC Number: 277-590-3. Physical State: neat. Solubility: Practically insoluble in water, freely soluble in acetone and in ethanol (96 per cent), sparingly soluble in propylene glycol. It shows polymorphism (5.9). Storage: Refrigerator. Applications: Prednicarbate is a medium potency topical corticosteroid used to manage pruritus and inflammation associated with responsive. skin conditions. Boiling Point: 640.7±55.0 °C(Predicted). Melting Point: 110-112°; mp 183°. Density: 1.25±0.1 g/cm3(Predicted). Product Description: Prednicarbate is a medium potency topical corticosteroid used to manage pruritus and inflammation associated with responsive. skin conditions. | |
| Prednicarbate Related Compound A | Prednicarbate Related Compound A. Uses: For analytical and research use. CAS No. 671225-26-6. Mole weight: 490.59. Catalog: AP671225266. | |
| Prednicarbate Related Compound B | Prednicarbate Related Compound B. Uses: For analytical and research use. CAS No. 104286-02-4. Mole weight: 432.51. EC Number: 600-552-8. Catalog: AP104286024. | |
| Prednicarbate Related Compound C | Prednicarbate Related Compound C. Uses: For analytical and research use. CAS No. 5740-62-5. Mole weight: 416.51. Catalog: AP5740625. | |
| Prednisolone | Prednisolone. Group: Biochemicals. Alternative Names: (11b)-11,17,21-Trihydroxy-pregna-1,4-diene-3,20-dione; Metacortandralone; Delta F. Grades: Highly Purified. CAS No. 50-24-8. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C21H28O5. US Biological Life Sciences. | Worldwide |
| Prednisolone | Prednisolone is a potent, orally active corticosteroid and a glucocorticoid. Prednisolone possesses about four times the anti-inflammatory activity of hydrocortisone while causing less salt and water retention. Prednisolone can be used for ocular, anti-inflammatory research[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 50-24-8. Pack Sizes: 10 mM * 1 mL in DMSO; 500 mg; 1 g; 5 g; 10 g; 25 g. Product ID: HY-17463. | |
| Prednisolone | 5g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C21H28O5. CAS No. 50-24-8. Prepack ID 12896812-5g. Molecular Weight 360.44. See USA prepack pricing. |  |
| Prednisolone 11,21-Diacetate | Prednisolone 11,21-Diacetate. Group: Biochemicals. Alternative Names: 11 β,17,21-Trihydroxypregna-1,4-diene-3,20-dione 11,21-Diacetate; (11 β)-11,21-Bis(acetyloxy)-17-hydroxy-pregna-1,4-diene-3,20-dione. Grades: Highly Purified. CAS No. 98523-85-4. Pack Sizes: 250mg. Molecular Formula: C25H32O7, Molecular Weight: 444.52. US Biological Life Sciences. | Worldwide |
| Prednisolone-17-ethylcarbonate | Prednisolone-17-ethylcarbonate. Alternative Names: (11β)-17-[(Ethoxycarbonyl)oxy]-11,21-dihydroxypregna-1,4-diene-3,20-dione. CAS No. 104286-02-4. Purity: 96%. Product ID: ACM104286024. Molecular formula: C24H32O7. Mole weight: 432.51. IUPAC Name: ethyl [(8S,9S,10R,11S,13S,14S,17R)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl] carbonate. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Prednisolone acetate | 5g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C23H30O6. CAS No. 52-21-1. Prepack ID 68026409-5g. Molecular Weight 402.48. See USA prepack pricing. | |
| Prednisolone acetate | Prednisolone acetate (Prednisolone 21-acetate) is an adrenocortical hormone active molecule with various pharmacological effects such as anti-inflammatory, anti-allergic, and immune suppression. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Prednisolone 21-acetate. CAS No. 52-21-1. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-B1214. | |
| Prednisolone acetate | Prednisolone acetate. Group: Biochemicals. Alternative Names: (11b). Grades: Highly Purified. CAS No. 52-21-1. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C23H30O6. US Biological Life Sciences. | Worldwide |
| Prednisolone Acetate | It belongs to the adrenocortical hormone and adrenocorticotropic hormone class, and is also widely used in the treatment of blood system diseases. CAS No. 125-10-0. Product ID: PAP-0083. Molecular formula: C23H28O6. Category: Hormone drug. Product Keywords: Hormone Series; Prednisolone Acetate; PAP-0083; Hormone drug; C23H28O6; 125-10-0. Appearance: Solid. Standard: BP/USP/EP. Color: White to Off-White. Physical State: Solid. Solubility: Chloroform (Slightly), Dioxane (Sparingly), DMSO (Slightly), Methanol (Slightly). Storage: Refrigerator. Applications: It is used to treat allergic, non-infectious skin diseases and some proliferative skin disorders. Boiling Point: 582.0±50.0 °C(Predicted). Melting Point: 240-242°C (dec.). Density: 1.28±0.1 g/cm3(Predicted). | |
| Prednisolone Acetate EP Impurity D | Prednisolone Acetate EP Impurity D. Uses: For analytical and research use. CAS No. 20423-99-8. Molecular formula: C21H28O4. Mole weight: 344.45. Catalog: APB20423998. | |
| Prednisolone Caproate | Prednisolone Caproate. Group: Biochemicals. Alternative Names: (11 β)-11,17-Dihydroxy-21-[(1-oxohexyl)oxy]-pregna-1,4-diene-3,20-dione; 11 β,17,21-Trihydroxypregna-1,4-diene-3,20-dione 21-Hexanoate. Grades: Highly Purified. CAS No. 69164-69-8. Pack Sizes: 250mg. Molecular Formula: C27H38O6, Molecular Weight: 458.59. US Biological Life Sciences. | Worldwide |
| Prednisolone disodium phosphate | Prednisolone disodium phosphate. Group: Biochemicals. Grades: Highly Purified. CAS No. 125-02-0. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C21H27Na2O8P. US Biological Life Sciences. | Worldwide |
| Prednisolone disodium phosphate | Prednisolone disodium phosphate is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties. Prednisolone disodium phosphate can be rapidly and completely hydrolyzed to Prednisolone in the plasma[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Prednisolone 21-phosphate disodium. CAS No. 125-02-0. Pack Sizes: 10 mM * 1 mL in Water; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0645. | |
| Prednisolone EP Impurity D | Prednisolone EP Impurity D. Uses: For analytical and research use. CAS No. 16355-29-6. Molecular formula: C21H28O6. Mole weight: 376.45. Catalog: APB16355296. | |
| Prednisolone EP Impurity E | Prednisolone EP Impurity E. Uses: For analytical and research use. CAS No. 95815-58-0. Molecular formula: C21H28O6. Mole weight: 376.45. Catalog: APB95815580. | |
| Prednisolone EP Impurity F | Prednisolone EP Impurity F. Uses: For analytical and research use. CAS No. 600-90-8. Molecular formula: C21H28O5. Mole weight: 360.45. Catalog: APB600908. | |
| Prednisolone EP Impurity G | Prednisolone EP Impurity G. Uses: For analytical and research use. CAS No. 2299-46-9. Molecular formula: C21H30O5. Mole weight: 362.47. Catalog: APB2299469. | |
| Prednisolone EP Impurity H | Prednisolone EP Impurity H. Uses: For analytical and research use. CAS No. 2427-64-7. Molecular formula: C21H26O5. Mole weight: 358.43. Catalog: APB2427647. | |
| Prednisolone EP Impurity I | Prednisolone EP Impurity I. Uses: For analytical and research use. CAS No. 13479-38-4. Molecular formula: C21H28O4. Mole weight: 344.45. Catalog: APB13479384. | |
| Prednisolone EP Impurity J | Prednisolone EP Impurity J. Uses: For analytical and research use. CAS No. 1807-14-3. Molecular formula: C21H28O4. Mole weight: 344.45. Catalog: APB1807143. | |
| Prednisolone Hemisuccinate | Prednisolone Hemisuccinate. Group: Biochemicals. Alternative Names: (11 β)-21-(3-Carboxy-1-oxopropoxy)-11,17-dihydroxy-pregna-1,4-diene-3,20-dione; Prednisolone 21-O- β-carbonylpropionic Acid; Prednisolone 21-hemisuccinate; Prednisolone 21-succinate; Prednisolone Bisuccinate; Prednisolone Succinate; Prednisolut; Δ1-Hydrocortisone 21-hemisuccinate. Grades: Highly Purified. CAS No. 2920-86-7. Pack Sizes: 1g. Molecular Formula: C25H32O8, Molecular Weight: 460.52. US Biological Life Sciences. | Worldwide |
| Prednisolone Hemisuccinate-d8 | Prednisolone Hemisuccinate-d8. Group: Biochemicals. Alternative Names: (11 β)-21-(3-Carboxy-1-oxopropoxy)-11,17-dihydroxy-pregna-1,4-diene-3,20-dione-d8; Prednisolone 21-O- β-carbonylpropionic Acid-d8; Prednisolone 21-hemisuccinate-d8; Prednisolone 21-succinate-d8; Prednisolone Bisuccinate-d8; Prednisolone Succinate-d8; Prednisolut; Δ1-Hydrocortisone 21-Hemisuccinate-d8. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C25H24D8O8, Molecular Weight: 468.57. US Biological Life Sciences. | Worldwide |
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